A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948126



Internal ID18594972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87430828..87500508hg38UCSC Ensembl
Innerchr10:89190585..89260265hg19UCSC Ensembl
Innerchr10:89180565..89250245hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3869681
hg1969681
hg1869681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1861594, nssv1861600, nssv1861602, nssv1861599, nssv1861596, nssv1861598, nssv1861597, nssv1861593, nssv1861595, nssv1861601
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948126
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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